| NDC Code | 35356-970-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (35356-970-90) |
|---|
| Product NDC | 35356-970 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glipizide And Metformin Hcl |
|---|
| Non-Proprietary Name | Glipizide And Metformin Hcl |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100629 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078728 |
|---|
| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
|---|
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 2.5; 250 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
|---|